Solvent Extraction Separation of Trivalent Lanthanide and Actinide Ions Using an Aqueous Aminomethanediphosphonic Acid

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Total Pages : 9 pages
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Book Synopsis Solvent Extraction Separation of Trivalent Lanthanide and Actinide Ions Using an Aqueous Aminomethanediphosphonic Acid by :

Download or read book Solvent Extraction Separation of Trivalent Lanthanide and Actinide Ions Using an Aqueous Aminomethanediphosphonic Acid written by and published by . This book was released on 1998 with total page 9 pages. Available in PDF, EPUB and Kindle. Book excerpt: The possibility of separating the trivalent lanthanides, represented by EU{sup 3+}, and actinides, represented by Cf{sup 3+}, using HDEHP in toluene and an aqueous phase containing N-piperidinomethane-1,1-diphosphotic acid, PMDPA, has been investigated. This modified aqueous phase offers potential advantages over the diethylenetriaminepentaacetic acid based TALSPEAK process because of the improved complexation properties of PMDPA in acidic solutions, and the ability to decompose PMDPA before disposal. Extraction experiments were conducted at 25 C in 2 M NaClO4 between -log [H] 1 and 2. The studies enabled us to derive the aqueous phase speciation, the stability constants of the aqueous complexes, and the Cf/Eu separation factors. Despite the presence of an amino group in PMDPA that should favor the retention of the actinides in the aqueous phase, the Cf/Eu separation factors are near unity under the conditions studied.

Separation of Trivalent Lanthanides and Actinides by Solvent Extraction Without Aqueous Complexing Agents

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Book Synopsis Separation of Trivalent Lanthanides and Actinides by Solvent Extraction Without Aqueous Complexing Agents by :

Download or read book Separation of Trivalent Lanthanides and Actinides by Solvent Extraction Without Aqueous Complexing Agents written by and published by . This book was released on 1976 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: A method of separating the trivalent actinides, mainly Am and Cm, from trivalent lanthanides is presented. This method embodies the sequential use of two different solvent extractants; the first extractant would remove the heavy lanthanides from the lighter lanthanides and Am--Cm, while the second would extract Am--Cm in preference to the lighter lanthanides. In this scheme, no additional complexing agents are required. Thus, waste disposal and corrosion problems are minimized. Overall separation factors for Am--Cm from lanthanide fission products in reactor wastes may be as high as several thousand. (auth).

The Solvent Extraction Separation of Trivalent Actinides from Lanthanides Using Aliquat 336-SCN

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Total Pages : 224 pages
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Book Synopsis The Solvent Extraction Separation of Trivalent Actinides from Lanthanides Using Aliquat 336-SCN by : Paul Vernon Beum

Download or read book The Solvent Extraction Separation of Trivalent Actinides from Lanthanides Using Aliquat 336-SCN written by Paul Vernon Beum and published by . This book was released on 1993 with total page 224 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Actinide Separations

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Total Pages : 632 pages
Book Rating : 4.:/5 (3 download)

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Book Synopsis Actinide Separations by : James D. Navratil

Download or read book Actinide Separations written by James D. Navratil and published by . This book was released on 1980 with total page 632 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Advances in Solvent Extraction

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ISBN 13 :
Total Pages : 324 pages
Book Rating : 4.6/5 (721 download)

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Book Synopsis Advances in Solvent Extraction by : Kevin L. Lyon

Download or read book Advances in Solvent Extraction written by Kevin L. Lyon and published by . This book was released on 2020 with total page 324 pages. Available in PDF, EPUB and Kindle. Book excerpt: Rare earth elements have become essential materials in advanced clean energy technologies and national security applications due to their unique properties. Despite their importance, the United States remains almost completely dependent upon foreign supply chains, notably imports from China, for both raw and finished commodities containing rare earth elements. This dissertation explores the implementation of a neutral ligand, N, N, N', N' tetraoctyl diglycolamide (TODGA), for the separation of rare earth elements. TODGA offers distinct advantages over traditional phosphonic acid extractants, notably the elimination of saponification to achieve high recovery in a solvent extraction circuit and improved adjacent lanthanide separation factors, ultimately requiring fewer solvent extraction stages to achieve high degrees of purity and recovery. This work marks the first use of TODGA's unique chemistry to separate and purify the rare earths from each other in hydrochloric acid media using counter-current solvent extraction.Chapter 1 introduces the concept of rare earths as a critical material and highlights historic and future challenges associated with the rare earth supply chain. Separations remains as one of the greatest challenges due to high capital and operating costs to purify individual rare earth elements, thus emphasizing the need for advances in solvent extraction to enable a viable domestic supply chain in the United States. Chapters 2 and 3 provide background context that motivated the research by describing commercial rare earth separation processes and an overview of TODGA's known applications and uses for trivalent lanthanide extraction and separation. While TODGA's lanthanide extraction chemistry has been studied extensively for separations relevant to the nuclear fuel cycle, it has not been successfully applied in the field of rare earth mining and hydrometallurgy to separate individual lanthanides with high degrees of recovery and purity in a continuous counter-current solvent extraction cascade. TODGA exhibits a unique extraction trend among "light" low molecular weight lanthanides, with an observed 50% increase in adjacent light lanthanide separation factors as compared to the industry standard phosphonic acid PC88A. This suggests that a counter-current solvent extraction cascade with a reduced number of stages may be implemented for the purification of light rare earth elements.Chapter 4 outlines the various experimental methods that were utilized to conduct this research. A variety of techniques were utilized in the approach, including laboratory batch equilibrium solvent extraction experiments, counter-current mixer-settler testing, and process modeling and simulation using MATLAB/Simulink.Chapter 5 provides the rationale behind counter-current solvent extraction modeling and simulation for process design. Mass balances around a solvent extraction cascade may be written as a system of ordinary differential equations and coupled with empirical laboratory equilibrium data to model the approach to steady state. Alternative techniques for steady state cascade modeling using algebraic equations written in the form of a tridiagonal matrix and solved using the Thomas Algorithm are discussed. This approach may also be coupled with empirical expressions for calculating distribution ratios as a function of free TODGA and aqueous phase chloride concentration at equilibrium.Chapter 6 describes experimental results that were used to evaluate the feasibility of TODGA's extraction chemistry in a counter-current solvent extraction circuit. While TODGA demonstrates improved light rare earth separation factors, they are still relatively low, implying that neighboring lanthanides essentially co-extract. Commercially, high degrees of purity and recovery are achieved by implementing a selective scrubbing technique through which the purified REE product stream is refluxed into the scrub section. Batch solvent extraction experiments and simplified counter-current solvent extraction experiments in mixer-settlers revealed that TODGA is indeed capable of selective scrubbing to purify REEs under proper solvent loading conditions.Chapter 7 describes the applied culmination of TODGA's extraction chemistry through the design and experimental testing of a solvent extraction process to produce the permanent magnet precursor material didymium (75% neodymium and 25% praseodymium by mass), from a mixed light rare earth chloride feed representative of that produced from the processing of bastnasite ore. The chapter includes single metal extraction data with empirically determined expressions for calculating distribution ratios, followed by batch counter-current extraction experiments for light REE separations. Batch experimental results were used to design a 24-stage counter-current solvent extraction cascade to purify PrNd from a mixture of La, Ce, Pr, and Nd. While experimental results of the cascade design did not achieve optimum recovery or purity, they indicate that TODGA can successfully be used to for the continuous separation and purification of light rare earths. Single metal distribution ratio correlations did not accurately model cascade behavior; a "pseudo single-metal" approach is presented to calculate distribution ratios under saturated loading conditions in a solvent extraction cascade.Chapter 8 discusses the implications of utilizing TODGA in an industrial setting. While the use of a neutral ligand has distinct benefits over phosphonic acids, there are several limitations to the solvent system that require additional research efforts to address. Furthermore, implementing TODGA chemistry has economic impacts that may potentially limit its commercial viability. Notable limitations discussed include organic phase loading capacity, ligand synthesis and production costs, and high molarity salt-bearing raffinate streams that must be recycled or disposed of. A structure/property relationship was identified for DGA extractants with varying alkyl chain substituents, indicating that short alkyl chains make stronger, more selective extractants but are prone to gelling and third phase formation. Longer alkyl chains maintain selectivity and slightly reduce overall extraction strength. Branched alkyl chains prevent gelling and third phase formation but comes at the cost of poor selectivity due to steric hindrance caused by the branched alkyl chains in the outer coordination sphere.Chapter 9 summarizes the general conclusion of this work: TODGA is capable of performing industrially relevant rare earth separations in continuous counter-current solvent extraction equipment, achieving high degrees of REE recovery and purity. However, its practical application is limited at this time due to its low organic phase loading. Ongoing research in collaboration with Oak Ridge National Laboratory is currently underway to synthesize and test novel DGA extractants with tailored alkyl chain substituents that achieve high degrees of organic phase loading capacity, maintain enhanced adjacent lanthanide selectivity among light rare earths, and demonstrate acceptable hydrodynamic behavior suitable for use in solvent extraction equipment.

Advanced Extraction Methods for Actinide

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Total Pages : pages
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Book Synopsis Advanced Extraction Methods for Actinide by :

Download or read book Advanced Extraction Methods for Actinide written by and published by . This book was released on 2005 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: The separation of An(III) ions from chemically similar Ln(III) ions is perhaps one of the most difficult problems encountered during the processing of nuclear waste. In the 3+ oxidation states, the metal ions have an identical charge and roughly the same ionic radius. They differ strictly in the relative energies of their f- and d-orbitals, and to separate these metal ions, ligands will need to be developed that take advantage of this small but important distinction. The extraction of uranium and plutonium from nitric acid solution can be performed quantitatively by the extraction with the TBP (tributyl phosphate). Commercially, this process has found wide use in the PUREX (plutonium uranium extraction) reprocessing method. The TRUEX (transuranium extraction) process is further used to coextract the trivalent lanthanides and actinides ions from HLLW generated during PUREX extraction. This method uses CMPO [(N, N-diisobutylcarbamoylmethyl) octylphenylphosphineoxide] intermixed with TBP as a synergistic agent. However, the final separation of trivalent actinides from trivalent lanthanides still remains a challenging task. In TRUEX nitric acid solution, the Am(III) ion is coordinated by three CMPO molecules and three nitrate anions. Taking inspiration from this data and previous work with calix[4]arene systems, researchers on this project have developed a C3-symmetric tris-CMPO ligand system using a triphenoxymethane platform as a base. The triphenoxymethane ligand systems have many advantages for the preparation of complex ligand systems. The compounds are very easy to prepare. The steric and solubility properties can be tuned through an extreme range by the inclusion of different alkoxy and alkyl groups such as methyoxy, ethoxy, t-butoxy, methyl, octyl, t-pentyl, or even t-pentyl at the ortho- and para-positions of the aryl rings. The triphenoxymethane ligand system shows promise as an improved extractant for both tetravalent and trivalent actinide recoveries form high level liquid wastes and a general actinide clean-up procedure. The selectivity of the standard extractant for tetravalent actinides, (N, N-diisobutylcarbamoylmethyl) octylphenylphosphineoxide (CMPO), was markedly improved by the attachment of three CMPO-like functions onto a triphenoxymethane platform, and a ligand that is both highly selective and effective for An(IV) ions was isolated. A 10 fold excess of ligand will remove virtually all of the 4+ actinides from the acidic layer without extracting appreciable quantities of An(III) and Ln(III) unlike simple CMPO ligands. Inspired by the success of the DIAMEX industrial process for extractions, three new tripodal chelates bearing three diglycolamide and thiodiglycolamide units precisely arranged on a triphenoxymethane platform have been synthesized for an highly efficient extraction of trivalent f-element cations from nitric acid media. A single equivalent of ligand will remove 80% of the Ln(III) ion from the acidic layer since the ligand is perfectly suited to accommodate the tricapped trigonal prismatic geometry preferred by the metal center. The ligand is perhaps the most efficient binder available for the heavier lanthanides and due to this unique attribute, the extraction event can be easily followed by 1H NMR spectroscopy confirming the formation of a TPP complex. The most lipophilic di-n-butyl tris-diglycolamide was found to be a significantly weaker extractant in comparison to the di-isopropyl analogs. The tris-thiodiglycolamide derivative proved to be an ineffective chelate for f-elements and demonstrated the importance of the etheric oxygens in the metal binding. The results presented herein clearly demonstrate a cooperative action of these three ligating groups within a single molecule, confirmed by composition and structure of the extracted complexes, and since actinides prefer to have high coordination numbers, the ligands should be particularly adept at binding with three arms. The use of such an extractant permits the extraction of metal ions form highly acidic environment through the ability of the compound to buffer the effect of high acid concentration. Stability toward hydrolysis and ease of synthesis and purification are additional favorable properties. The ligands describe above based on the triphenoxymethane platform are not only easily available in large quantities but also amenable to nearly unlimited chemical modifications. Finally, with this platform, two highly effective ligands incorporating CMPO and glycoldiamide moieties have been prepared and fully characterized, and both examples are perhaps the most efficient and selective examples of these important classes of ligands. Continued refinements of these systems have the potentially further improve the selectivity and affinity for An(III) ions.

Characterizing Mixed Ligand F-Element Complexes for Improved Actinide(III)/Lanthanide(III) Separations

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Total Pages : 206 pages
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Book Synopsis Characterizing Mixed Ligand F-Element Complexes for Improved Actinide(III)/Lanthanide(III) Separations by : Ian Michael Hobbs

Download or read book Characterizing Mixed Ligand F-Element Complexes for Improved Actinide(III)/Lanthanide(III) Separations written by Ian Michael Hobbs and published by . This book was released on 2017 with total page 206 pages. Available in PDF, EPUB and Kindle. Book excerpt: Seaborg and coworkers established in the 1950s that the most effective approach to accomplishing a lanthanide trivalent actinide group separation was to introduce donor atoms softer than oxygen, specifically Cl-- , into a low selectivity separation platform like Dowex 50 cation exchange resin. This soft-donor effect was attributed to the slightly stronger covalent contribution in the bonding of actinides to such ligands. A decade later, Weaver and Kappelmann developed the TALSPEAK concept, based on the introduction of multiple N-donor holdback reagents, like DTPA (diethylenetriamine pentaacetic acid) to accomplish a similar separation. Though the chemistry of TALSPEAK is more complex than the soft donor-cation exchange separation, it did enable a potentially high throughput countercurrent solvent extraction approach to An(III)/Ln(III) separations with high separation factors. Because the covalency effect is relatively weak (7--8% increased bonding affinity for An(III) over similarly-sized Ln(III)), the adoption of reagents with more N-donor atoms increases separation efficiency. However, the octadentate DTPA suffers from some issues arising from the comparatively slow complexation/decomplexation kinetics of complex molecules. In the Advanced TALSPEAK system, the primary aqueous holdback reagent is HEDTA ((2 hyroxyethyl)ethylenediaminetriacetic acid), a pentadentate aminopolycarboxylate ligand, with three water molecules completing the cation coordination environment. The Ln(HEDTA)(OH2) 3 aqueous complex leaves room for the addition of a secondary soft donor ligand, for example iminodiacetic acid. In this report, selected results of an investigation of the thermodynamics and kinetics of such ternary complexes and their impact on Advanced TALSPEAK separations will be described.

Engineering for Nuclear Fuel Reprocessing

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ISBN 13 :
Total Pages : 1044 pages
Book Rating : 4.3/5 (91 download)

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Book Synopsis Engineering for Nuclear Fuel Reprocessing by : Justin T. Long

Download or read book Engineering for Nuclear Fuel Reprocessing written by Justin T. Long and published by . This book was released on 1967 with total page 1044 pages. Available in PDF, EPUB and Kindle. Book excerpt: